Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_assertion description "[These data suggest AMPD2-related PCH as a potentially treatable early-onset neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_assertion evidence source_evidence_literature NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_assertion SIO_000772 23911318 NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_assertion wasDerivedFrom befree-20150227 NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_assertion wasGeneratedBy ECO_0000203 NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP237697.RA4ZRKYZS6oW9H_e7IeCYOaT8hgDDzEE1TxwtToJknIGM130_provenance.